Clinitron Air Fluidized Bed Manual
Ethos offers the best in-home Air Fluidized Therapy (AFT) technologies for patients recovering from wounds or pressure injuries. AFT, also known as a bead bed or sand bed, is considered the gold standard for treating Stage III and IV pressure ulcers and can be critical to accelerate wound healing.
Air Fluidized Therapy Products
Clinitron® Rite Hite®
Clinitron At Home ®
AirusTM
Manually delete snapshots parallels version. Clinitron Air Fluidized Bed Manual This article describes a patient with a Stage IV pressure ulcer who was started on Clinitron therapy. A wound healing rate of 67% was achieved within a month of therapy and 99% after 104 days of Clinitron air-fluidized therapy. An experienced home healthcare clinician expected that a. CLINITRON BED BED, AIR FLUIDIZED: Back to Search Results: Model Number 0800: Device Problems Loss of Power (1475); Device Displays Incorrect Message (2591) Patient Problem Injury (2348) Event Date: Event Type Injury Event Description Hill-rom received a report from the account stating the unit was alarming and shutting down.
How Air Fluidized Therapy Works
Air Fluidized Therapy is proven to be one of the best technologies to help wounds heal faster. With AFT, the bed is filled with silicone beads and warm filtered air, providing a fluid-like flotation that gently flows around the patient. AFT relieves pressure on wound sites, allowing for increased capillary blood flow. The technology is designed to maintain a cleaner, more comfortable micro-environment to inhibit bacterial growth.
Product Details
Clinitron Rite Hite
AIR FLUIDIZED THERAPY
- Hybrid bed features low air loss therapy and articulating frame.
- Head articulation provides ideal surface for patients requiring pulmonary positioning in combination with turning and repositioning.
- Simulated fluid environment provides lower interface pressure and superior management of the patient’s microclimate.
- Hi/Lo feature provides height adjustment and allows for easier patient egress and safe working height for caregivers.
- Product Specifications
- Patient Weight Limit 350 LBS.
Length
Width
- Sleep Surface
- 36 inches
- Overall
- 42 inches
Height
Clinitron At Home
Air Fluidized Therapy
- Immersion into simulated fluid environment allows for lower interface pressure, helps reduce friction and shear and manage the patient’s microclimate.
- Articulating frame with low air loss provides the ideal solution for patients requiring immediate or frequent changes in body positioning.
- Modular design allows the therapy to fit easily in most home care environments.
- Height adjustment using 4 inch spacers allows adjustment to aide patient egress or to offer a safe working height for caregivers.
- Product Specifications
- Patient Weight Limit 350 LBS.
Length
Width
- Sleep Surface
- 34 inches
- Overall
- 41 inches
Height
- Lowest
- 26 inches
- Maximum Ht. w/2 spacers
- 34.5 inches
- spacers (each)
- 4 inches
AIRUS
AIR FLUIDIZED THERAPY
- Allows for full body contact with fluidized microspheres making it the ideal solution for patients with upper body pressure injuries, post flap and graft surgery.
- Hand and Foot Controls turn fluidization on and off to assist with patient care.
- Foam Backrest allows for 30-degree head elevation.
- Battery Back-up allows for intermittent fluidization for up to two hours.
- Product Specifications
- Patient Weight Limit 350 LBS.
Length
Width
- Sleep Surface
- 32 inches
- Overall
- 36 inches
Height
- Lowest
- 26 inches
- Maximum Ht. w/Wheel Carriage
- 33 inches
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| 510(k) | | DeNovo | | Registration & Listing | | Adverse Events | | Recalls | | PMA | | HDE | | Classification | | Standards |
| CFR Title 21 | | Radiation-Emitting Products | | X-Ray Assembler | | Medsun Reports | | CLIA | | TPLC |
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| HILL-ROM BATESVILLE CLINITRON RITEHITE C-8 ASSY BED, AIR FLUIDIZED | Back to Search Results |
| | Model Number P0800010019 | | Device Problem Insufficient Information (3190) | | Patient Problem Skin Erosion (2075) | | Event Date 08/10/2017 | | Event Type Injury | | Manufacturer Narrative | The hill-rom technician found the proportional valve needed to be replaced. The technician replaced the proportional valve to resolve the issue. The patient was evaluated by the hospital nursing staff and found to have a sacral wound that had progressed from a stage 2 to a stage 3, as well as 3 wounds on her left foot toes at a stage 2 and 1 on the fifth toe at a stage 1. The patient was treated with wet to dry dressings, santyl ointment, hydrogel and skin prep. Development of pressure ulcers is multifactorial and cannot be only attributed to performance of the surface. Siemens sensation 4 technical manuals. Risk factors include protein-calorie malnutrition, microclimate (skin wetness caused by sweating or incontinence), diseases that reduce blood flow to the skin, such as arteriosclerosis, or diseases that reduce the sensation in the skin, such as paralysis or neuropathy. Position changes are key to pressure sore prevention and treatment. These changes need to be frequent, repositioning needs to avoid stress on the skin, and body positions need to minimize the risk of pressure on vulnerable areas. Per the hill-rom user manual, poor fluidization; if fluidization is sluggish or uneven, notify your hill-rom representative. Fluidization is affected by the following: room temperature, humidity, the amount of materials, such as fluid, cells or cellular debris, which has escaped from the blood vessels and has been deposited in tissues or on tissue surfaces, restricted air circulation from blankets on the bed. A search of the hill-rom maintenance records showed hill-rom performed preventative maintenance on this bed in 2017. It is unknown if the facility performed any other preventative maintenance on this bed. Based on this information, no further action is required. | | Event Description | Hill-rom received a report from the account stating the patient's sacral wound had worsened from a stage 2 to stage 3. The bed was located at the account. There was a patient injury reported. This report was filed in our complaint handling system as complaint #(b)(4). | | Search Alerts/Recalls |
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Positioning Patient On Clinitron Bed
| New Search Submit an Adverse Event Report |
Clinitron Air Fluidized Bed Price
| Type of Device | BED, AIR FLUIDIZED |
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| Manufacturer (Section D) | | HILL-ROM BATESVILLE | | 1069 state route 46 east | | batesville IN 47006 |
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| Manufacturer Contact | | erin padgett | | 1069 state route 46 east | | batesville, IN 47006 | | 8129312791 |
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| MDR Report Key | 6820221 |
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| MDR Text Key | 83637912 |
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| Report Number | 1824206-2017-00352 |
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| Device Sequence Number | 1 |
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| Product Code | INX |
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| Combination Product (Y/N) | N |
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| Reporter Country Code | US |
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| PMA/PMN Number | K964223 |
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| Number of Events Reported | 1 |
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| Summary Report (Y/N) | N |
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| Report Source | Manufacturer |
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| Source Type | COMPANY REPRESENTATIVE,USER F |
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| Reporter Occupation |
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| Type of Report | Initial |
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| Report Date | 08/10/2017 |
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| 1 Device Was Involved in the Event |
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| 1 Patient Was Involved in the Event |
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| Date FDA Received | 08/25/2017 |
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| Is This An Adverse Event Report? | Yes |
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| Is This A Product Problem Report? | No |
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| Device Operator | OTHER CAREGIVERS |
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| Device MODEL Number | P0800010019 |
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| Was Device Available For Evaluation? | Yes |
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| Is The Reporter A Health Professional? | Yes |
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| Was the Report Sent to FDA? |
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| Event Location | No Information |
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| Date Manufacturer Received | 08/10/2017 |
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| Was Device Evaluated By Manufacturer? | Yes |
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| Date Device Manufactured | 06/05/2007 |
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| Is The Device Single Use? | No |
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| Is this a Reprocessed and Reused Single-Use Device? | No |
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| Type of Device Usage | Unkown |
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| Patient TREATMENT DATA |
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| Date Received: 08/25/2017 Patient Sequence Number: 1 |
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